tert-butyl ((1r,4r)-4-((2-(1H-indol-4-yl)-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)methyl)cyclohexyl)carbamate

Base Information

Chemical Name:tert-butyl ((1r,4r)-4-((2-(1H-indol-4-yl)-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)methyl)cyclohexyl)carbamate
CAS No.:1394072-66-2
Molecular Formula:C₂₉H₃₈N₆O₃
Molecular Weight:518.659
Hs Code.:

Synonyms:tert-butyl ((1r,4r)-4-((2-(1H-indol-4-yl)-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)methyl)cyclohexyl)carbamate

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Chemical Property of tert-butyl ((1r,4r)-4-((2-(1H-indol-4-yl)-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)methyl)cyclohexyl)carbamate

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Technology Process of tert-butyl ((1r,4r)-4-((2-(1H-indol-4-yl)-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)methyl)cyclohexyl)carbamate

There total 3 articles about tert-butyl ((1r,4r)-4-((2-(1H-indol-4-yl)-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)methyl)cyclohexyl)carbamate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 5.4%

: 1394070-70-2
tert-butyl (1R,4R)-4-((2-chloro-6a,7,9,10-tetrahydro-[1,4]oxazin[3,4-h]pteridin-5(6H)-yl)methyl)cyclohexylcarbamate

: 220465-43-0
indole-4-boronic acid

: 1394072-66-2
tert-butyl ((1r,4r)-4-((2-(1H-indol-4-yl)-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)methyl)cyclohexyl)carbamate

Guidance literature:: With sodium hydrogencarbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; water; at 100 ℃; for 1h; microwave irradiation;

Reference yield:

: 1268474-50-5
2-chloro-6a,7,9,10-tetrahydro[1,4]oxazino[3,4-h]pteridin -6(5H)-one

: 1394072-66-2
tert-butyl ((1r,4r)-4-((2-(1H-indol-4-yl)-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)methyl)cyclohexyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C

2: potassium tert-butylate / ISOPROPYLAMIDE / 85 °C

3: sodium hydrogencarbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 1 h / 100 °C / microwave irradiation

With lithium aluminium tetrahydride; potassium tert-butylate; sodium hydrogencarbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; 1,4-dioxane; ISOPROPYLAMIDE; water;

Reference yield:

: 1394070-48-4
2-chloro-5,6,6a,7,9,10-hexahydro-[1,4]oxazino[3,4-h]pteridine

: 1394072-66-2
tert-butyl ((1r,4r)-4-((2-(1H-indol-4-yl)-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)methyl)cyclohexyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium tert-butylate / ISOPROPYLAMIDE / 85 °C

2: sodium hydrogencarbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 1 h / 100 °C / microwave irradiation

With potassium tert-butylate; sodium hydrogencarbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; ISOPROPYLAMIDE; water;